Rietschel M - Search Results

1

Investigation of blood mRNA biomarkers for suicidality in an independent sample.

Mullins N, Hodgson K, Tansey KE, Perroud N, Maier W, Mors O, Rietschel M, Hauser J, Henigsberg N, Souery D, Aitchison K, Farmer A, McGuffin P, Breen G, Uher R, Lewis CM. Mullins N, et al. Among authors: rietschel m. Transl Psychiatry. 2014 Oct 28;4(10):e474. doi: 10.1038/tp.2014.112. Transl Psychiatry. 2014. PMID: 25350297 Free PMC article.

2

[Genetic association in psychiatric diseases. Concepts and findings].

Propping P, Nöthen MM, Körner J, Rietschel M, Maier W. Propping P, et al. Among authors: rietschel m. Nervenarzt. 1994 Nov;65(11):725-40. Nervenarzt. 1994. PMID: 7816149 Review. German. No abstract available.

3

Assessing the statistical power to detect linkage in a sample of 51 bipolar affective disorder pedigrees.

Lim LC, Craddock N, Owen M, Sham P, Nöthen MM, Körner J, Rietschel M, Fimmer R, Propping P, McGuffin P, Murray R, Gill M. Lim LC, et al. Among authors: rietschel m. Behav Genet. 1996 Mar;26(2):113-22. doi: 10.1007/BF02359889. Behav Genet. 1996. PMID: 8639147

4

Systematic screening for mutations in the human serotonin 1F receptor gene in patients with bipolar affective disorder and schizophrenia.

Shimron-Abarbanell D, Harms H, Erdmann J, Albus M, Maier W, Rietschel M, Körner J, Weigelt B, Franzek E, Sander T, Knapp M, Propping P, Nöthen MM. Shimron-Abarbanell D, et al. Among authors: rietschel m. Am J Med Genet. 1996 Apr 9;67(2):225-8. doi: 10.1002/(SICI)1096-8628(19960409)67:2<225::AID-AJMG16>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8723053

5

Dopamine D3 receptor Gly9/Ser9 polymorphism and schizophrenia: no increased frequency of homozygosity in German familial cases.

Rietschel M, Nöthen MM, Albus M, Maier W, Minges J, Bondy B, Körner J, Hemmer S, Fimmers R, Möller HJ, Wildenauer D, Propping P. Rietschel M, et al. Schizophr Res. 1996 May;20(1-2):181-6. doi: 10.1016/0920-9964(95)00074-7. Schizophr Res. 1996. PMID: 8794508

6

The human serotonin 7 (5-HT7) receptor gene: genomic organization and systematic mutation screening in schizophrenia and bipolar affective disorder.

Erdmann J, Nöthen MM, Shimron-Abarbanell D, Rietschel M, Albus M, Borrmann M, Maier W, Franzek E, Körner J, Weigelt B, Fimmers R, Propping P. Erdmann J, et al. Among authors: rietschel m. Mol Psychiatry. 1996 Nov;1(5):392-7. Mol Psychiatry. 1996. PMID: 9154233

7

Investigation of complement C4B deficiency in schizophrenia.

Schroers R, Nöthen MM, Rietschel M, Albus M, Maier W, Schwab S, Wildenauer D, Fimmers R, Propping P, Dewald G. Schroers R, et al. Among authors: rietschel m. Hum Hered. 1997 Sep-Oct;47(5):279-82. doi: 10.1159/000154424. Hum Hered. 1997. PMID: 9358016

8

Adenosine A1 receptor and bipolar affective disorder: systematic screening of the gene and association studies.

Deckert J, Nöthen MM, Albus M, Franzek E, Rietschel M, Ren H, Stiles GL, Knapp M, Weigelt B, Maier W, Beckmann H, Propping P. Deckert J, et al. Among authors: rietschel m. Am J Med Genet. 1998 Feb 7;81(1):18-23. doi: 10.1002/(sici)1096-8628(19980207)81:1<18::aid-ajmg4>3.0.co;2-j. Am J Med Genet. 1998. PMID: 9514582

9

Further evidence for a susceptibility locus on chromosome 10p14-p11 in 72 families with schizophrenia by nonparametric linkage analysis.

Schwab SG, Hallmayer J, Albus M, Lerer B, Hanses C, Kanyas K, Segman R, Borrman M, Dreikorn B, Lichtermann D, Rietschel M, Trixler M, Maier W, Wildenauer DB. Schwab SG, et al. Among authors: rietschel m. Am J Med Genet. 1998 Jul 10;81(4):302-7. Am J Med Genet. 1998. PMID: 9674975

10

Analysis of a polymorphism in the tuberous sclerosis (TSC2) gene does not predispose to schizophrenia.

Przkora R, Falkai P, von Deimling A, Wiestler OD, Albus M, Rietschel M, Maier W, Bayer TA. Przkora R, et al. Among authors: rietschel m. Eur Arch Psychiatry Clin Neurosci. 1998;248(6):314-5. doi: 10.1007/s004060050056. Eur Arch Psychiatry Clin Neurosci. 1998. PMID: 9928911 Clinical Trial.

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